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NOSIP, a novel modulator of endothelial nitric oxide synthase activity

DEDIO, JÜRGEN, KÖNIG, PETER, WOHLFART, PAULUS, SCHROEDER, CHRISTIAN, KUMMER, WOLFGANG, MÜLLER-ESTERL, WERNER·2001·The FASEB Journal

Abstract

Production of nitric oxide (NO) in endothelial cells is regulated by direct interactions of endothelial nitric oxide synthase (eNOS) with effector proteins such as Ca 2+ ‐calmodulin, by posttranslational modifications such as phosphorylation via protein kinase B, and by translocation of the enzyme from the plasma membrane caveolae to intracellular compartments. Reversible acylation of eNOS is thought to contribute to the intracellular trafficking of the enzyme;however, protein factor(s) that govern the translocation of the enzyme are still unknown. Here we have used the yeast two‐hybrid system and identified a novel 34 kDa protein, termed NOSIP (eNOS interacting protein), which avidly binds to the carboxyl‐terminal region of the eNOS oxygenase domain. Coimmunoprecipitation studies demonstrated the specific interaction of eNOS and NOSIP in vitro and in vivo , and complex formation was inhibited by a synthetic peptide of the caveolin‐1 scaffolding domain. NO production was significantly reduced in eNOS‐expressing CHO cells (CHO‐eNOS) that transiently overexpressed NOSIP. Stimulation with the calcium ionophore A23187 induced the reversible translocation of eNOS from the detergentinsoluble to the detergent‐soluble fractions of CHO‐eNOS, and this translocation was completelyprevented by transient coexpression of NOSIP in CHO‐eNOS. Immunofluorescence studies revealed a prominent plasma membrane staining for eNOS in CHO‐eNOS that was abolished in the presence of NOSIP. Subcellular fractionation studies identified eNOS in the caveolin‐rich membrane fractions of CHO‐eNOS, and coexpression of NOSIP caused a shift of eNOS to intracellular compartments. We conclude that NOSIP is a novel type of modulator that promotes translocation of eNOS from the plasma membrane to intracellular sites, thereby uncoupling eNOS from plasma membrane caveolae and inhibiting NO synthesis.—Dedio, J., König, P., Wohlfart, P., Schroeder, C., Kummer, W., Muller‐Esterl, W. NOSIP, a novel modulator of endothelial nitric oxide synthase activity. FASEB J. 15, 79–89 (2001)

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Metadata

Authors
DEDIO, J., KÖNIG, P., WOHLFART, P., SCHROEDER, C., KUMMER, W., & MÜLLER-ESTERL, W.
Venue
The FASEB Journal
Publisher
Wiley
Published
2001-01
Volume
15
Issue
1
Pages
79-89
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W2003801493
Cited by
191
References
3
FWCI
7.37
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: NOSIP, a novel modulator of endothelial nitric oxide synthase activity. https://app.cochat.ai/papers/10.1096/fj.00-0078com
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DEDIO, J., KÖNIG, P., WOHLFART, P., SCHROEDER, C., KUMMER, W., & MÜLLER-ESTERL, W. (2001). NOSIP, a novel modulator of endothelial nitric oxide synthase activity. The FASEB Journal. https://doi.org/10.1096/fj.00-0078com

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